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Craniofacial Dysostosis

Known as: Crouzon disease, syndrome crouzon's, crouzon's syndrome 
A syndrome inherited in an autosomal dominant pattern. It is characterized by early fusion of the bones of the skull and face. Patients have a… 
National Institutes of Health

Related topics

Related topics

26 relations
Aarskog syndromeAcrocephalosyndactyliaApert-Crouzon DiseaseConnective and Soft Tissue

Narrower (10)

Bazopoulou Kyrkanidou syndromeCROUZON SYNDROME WITH ACANTHOSIS NIGRICANS (disorder)Craniofacial Dysostosis with Diaphyseal HyperplasiaCraniofacial dysostosis type 1

Broader (1)

Hereditary Diseases

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2010
Review
2010
Ocular Manifestations of Apert and Crouzon Syndromes: Qualitative and Quantitative Findings
There are significant differences in the ocular manifestations of Apert and Crouzon syndromes. Here, we present qualitative and… 
Review
2005
Review
2005
Apert and Crouzon Syndromes: Clinical Findings, Genes and Extracellular Matrix
Apert and Crouzon syndromes are well known craniostenosis. In the last 10 years several studies were performed to provide a… 
Highly Cited
2004
Highly Cited
2004
Ror2 knockout mouse as a model for the developmental pathology of autosomal recessive Robinow syndrome
Robinow syndrome (RS) is a human dwarfism syndrome characterized by mesomelic limb shortening, vertebral and craniofacial… 
Highly Cited
1999
Highly Cited
1999
Airway obstruction in severe syndromic craniosynostosis.
Airway obstruction is frequent in patients with severe syndromic craniosynostosis, and must be treated for successful, complete… 
Highly Cited
1995
Highly Cited
1995
Monobloc craniomaxillofacial distraction osteogenesis in a newborn with severe craniofacial synostosis: a preliminary report.
Severe craniofacial synostosis can be a devastating problem for a newborn infant. Reasons for early surgical intervention include… 
Highly Cited
1989
Highly Cited
1989
Microvascular surgery as an adjunct to craniomaxillofacial reconstruction.
Highly Cited
1988
Highly Cited
1988
Legless, a novel mutation found in PHT1-1 transgenic mice.
In this report it is shown that the PHT1-1 line of transgenic mice exhibited a pattern of developmental abnormalities when the… 
Highly Cited
1986
Highly Cited
1986
Vascularized Outer‐Table Calvarial Bone Flaps
Based on an anatomic study of the vascularization of the calvarium in cadavers, a technique for the transfer of vascularized… 
Highly Cited
1985
Highly Cited
1985
CT of dry skulls with craniofacial deformities: accuracy of three-dimensional reconstruction.
Dry skulls from patients with Crouzon syndrome or orbital neurofibromatosis were studied using three-dimensional reconstruction… 
Highly Cited
1975
Highly Cited
1975
Middle-third facial osteotomies: their use in the correction of acquired and developmental dentofacial and craniofacial deformities.
: A method to describe middle-third dentofacial and craniofacial deformities systematically and more specifically is presented… 
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